Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Complex symmetry

DNA viruses Poxviruses Variola Vaccinia Large particles 200 x 250nm complex symmetry Variola is the smallpox virus. It produces a systemic infection with a characteristic vesicular rash affecting the face, arms and legs, and has a high mortality rate. Vaccinia has been derived from the cowpox virus and is used to immunize against smallpox... [Pg.63]

The (OCS)2 anion is the next logical system, taking us into the realm of polyatomic anions with rich photochemistry and more complex symmetry. (OCS)2 is an example of how dramatically the properties of a compound (e.g., carbonyl sulfide) may change upon electron capture and/or solvation. . .. [Pg.460]

For Cu(II) square-planar complexes, B2g is the ground state, whereas for V02+ complexes (symmetry C4v), the ground state is Bu which is the same as the Big function in Eq. (131). For V02+ complexes, the only changes required in Eq. (131) are that the MO coefficients be different for orbitals of atoms 5 and 6. We shall first consider the case where B is the ground state. [Pg.144]

The simplest symmetry operations and elements needed to describe unitcell symmetry are translation, rotation (element rotation axis), and reflection (element mirror plane). Combinations of these elements produce more complex symmetry elements, including centers of symmetry, screw axes, and glide planes (discussed later). Because proteins are inherently asymmetric, mirror planes and more complex elements involving them are not found in unit cells of proteins. All symmetry elements in protein crystals are translations, rotations, and screw axes, which are rotations and translations combined. [Pg.62]

E. Brandas, Complex Symmetry, Jordan Blocks and Microscopic Selforganization An Examination of the Limits of Quantum Theory Based on Nonself-adjoint Extensions with Illustrations from Chemistry and Physics, in N. Russo, V. Ya. Antonchenko, E. Kryachko (Eds.), Self-Organization of Molecular Systems From Molecules and Clusters to Nanotubes and Proteins, NATO Science for Peace and Security Series A Chemistry and Biology, Springer Science+Business Media B.V., Dordrecht, 2009, p. 49. [Pg.111]

Even if the equations arrived at seem familiar there are some obvious fundamental differences. First of all, the ansatz singles out two mirror spaces, where the particle and its mirror image may be located, respectively. Second, the expanded complex symmetric representation takes into account complex resonance states. Note also, as said above, that the complex symmetry can be obtained from the hermitean representation via a non-positive definite metric, i.e. [Pg.119]

Invariance Property of "Complex Symmetry" under Restricted Similarity Transformations. [Pg.186]

Invariance of the Property of "Complex Symmetry" under Restricted Similarity Transformations.- Starting from the general similarity transformation (3.1), one obtains the two relations... [Pg.211]

Perdeuteration of transition metal complexes, such as [Rh(bpy)3], [Ru(bpy) [Os(bpy)3] +, Pt(2-thpy)2, etc. leaves the complex symmetry usually unchanged. Nevertheless, a number of characteristic effects can be observed ... [Pg.157]

The dominating peak at 23,150 cm with a halfwidth of 650 cm (Figs. 28 and 29) corresponds obviously to the peak found in the absorption spectrum of Fig. 12 near 23,800 cm (= 420 nm) with a molar extinction coefficient of = 10,7001/mol cm [145]. The corresponding electronic state has been classified in Ref. [53] as a MLCT state. Due to the ab initio study of Ref. [66] the state is assigned to the second singlet that has also dominant MLCT character. The CASPT2 calculations place this state to 23,450 cm In a C2V complex symmetry, this second singlet is classified as 63 [66]. [Pg.169]

Symmetry operations, therefore, can be visualized by means of certain symmetry elements represented by various graphical objects. There are four so-called simple symmetry elements a point to visualize inversion, a line for rotation, a plane for reflection and the already mentioned translation is also a simple symmetry element, which can be visualized as a vector. Simple symmetry elements may be combined with one another producing complex symmetry elements that include roto-inversion axes, screw axes and glide planes. [Pg.9]

Complex symmetry elements are shown in Table 1.3. There are three new complex symmetry elements, which are listed in italics in this table ... [Pg.10]

No new complex symmetry element is formed as a result of this combination. [Pg.11]

Earlier (see Figure 1.7) we established that there are four simple symmetry operations, namely rotation, reflection, inversion and translation. Among the four, reflection in a mirror plane may be represented as a complex symmetry element - two-fold inversion axis - which includes simultaneous two-fold rotation and inversion. Therefore, in order to minimize the number of simple symmetry operations, we will begin with rotation, inversion and translation, noting that complex operations can be described as simultaneous applications of these three simple transformations. [Pg.72]

Tetrahedral complexes are formed with water and ammonia. Schematically, the complex symmetries qualitatively explaining the observed spectral changes are represented by the following diagram, although some uncertainty remains as to the number of ligands in the aquo- and ammo-complexes. [Pg.493]

By hydrogenation of Ba-Cu alloys at 10 bar H2 pressure and room temperature, followed by annealing at 643 K under 160 bar H2 pressure dark brownish powder sensitive to air and moisture ordered structure (Figure 35) from npd on deuteride Pile, Z = 2 contains distorted 18-electron tet-[CuD4] complexes (symmetry 1) surrounded by nine Ba (three sites) in ttp configuration seven D sites, of which three anionic D tetrahedral surrounded by four M + lif 7Ba2+.3[CuH4] -.5H- Cu di°. [Pg.1553]

It is important that the acceleration of the H-D exchange, observed experimentally on the replacement of the PtCl/ or Pt(H20)4 catalysts by PtClaCH O), could not be related to any calculated quantum-chemical parameters. It was therefore postulated that an optimum combination of the donor-acceptor and dative mechanisms of the transfer of electron density is essential for the effective alkane-platinum(II) complex interaction. Since the contribution of the former inaeases and that of the latter diminishes with the increase of the positive charge on the complex, the optimum combination can be achieved for the complex with zero charge. Somewhat earlier, the presence of a catalytic activity maximum for the complex PtCl2(H20)2 was attributed to the influence of the symmetry of the ligand environment [32]. On the basis of the hypothesis that the formation of a bond with the activated alkane takes place mainly on interaction with the drf AO of the complex, the rates of reaction were correlated with the contribution by this orbital to the LUMO of the platinum(II) complex. Symmetry considerations led to the conclusion that, for n = 0 and n = 4, the LUMO of the complex is formed solely by the AO and cannot contain an admixture of the dfl state. As a consequence of the decrease of symmetry for n =1, 2, 3, such an admixture exists but the n = 2 complex occupies a special place (thus the... [Pg.291]

Line widths are of reasonable magnitudes for Mo spectra, except in those extreme cases of high solvent viscosity, very large molecules or smaller molecules which suffer severe steric crowding and distortion, and unusually unsymmetrical electronic environments at the metal centre. Reasons given for broader than theoretically expected line widths have been based on short relaxation times, decreased electronic and complex symmetry, the... [Pg.197]

Keywords Klein-Gordon equation Maxwell s equation Complex symmetry Jordan blocks Special and general relativity Electromagnetic and gravitational fields Schwarzschild radius... [Pg.73]

We start our analysis by building up the valence orbitals of 18.13 in terms of a C21, Pe(CO)3 fragment and two ethylcnes. Notice that the olefins lie in the equatorial plane. This, recall from Section 17.3, is the electronically preferred way to orient olefins in a trigonal bipyramidal complex. Symmetry-adapted linear combinations of the n and ti - levels of the ethylcnes are shown in 18,17 to 18.20... [Pg.344]


See other pages where Complex symmetry is mentioned: [Pg.318]    [Pg.84]    [Pg.399]    [Pg.612]    [Pg.399]    [Pg.7]    [Pg.64]    [Pg.322]    [Pg.1554]    [Pg.221]    [Pg.167]    [Pg.547]    [Pg.49]    [Pg.11]    [Pg.11]    [Pg.14]    [Pg.20]    [Pg.949]    [Pg.33]    [Pg.290]    [Pg.9]    [Pg.229]    [Pg.391]    [Pg.78]    [Pg.211]    [Pg.445]    [Pg.146]   
See also in sourсe #XX -- [ Pg.78 ]

See also in sourсe #XX -- [ Pg.4 , Pg.5 , Pg.6 , Pg.10 , Pg.11 , Pg.20 , Pg.21 ]

See also in sourсe #XX -- [ Pg.12 , Pg.16 , Pg.17 , Pg.19 , Pg.21 , Pg.23 , Pg.24 , Pg.27 ]




SEARCH



Chromium complexes, absorption symmetry

Complex ions, symmetry

Design of Low Symmetry Complexes

Iron complexes high symmetry

Olefin complexes symmetry considerations

Symmetry element complex

Symmetry in complexes

Symmetry of complexes

Symmetry reduction five-coordinate complexes

Tetragonal symmetry complexes

Transition-group complexes, forbidden transitions symmetry

© 2024 chempedia.info